Showing results (241-250 of 311) with videos related to

Sort By:
Pageof 32
Journal De Genetique Humaine|August 1, 1988
[Alpha-fetoprotein and trisomy 21]S Guibaud, C Boisson, A Simplot, et al.
Chirurgie Pediatrique|January 1, 1989
[Congenital mega-urethra. Comments apropos of a case report]H Dodat, P Takvorian, P Cochat, et al.
Pediatric Transplantation|March 22, 2001
Fading renal hyperfiltration in children following liver transplantationM Schell, A Lachaux, A Hadj-Aïssa, et al.
Pediatrie|January 1, 1989
[Familial infantile nephrotic syndrome with ocular abnormalities]C Glastre, P Cochat, S Colon, et al.
Pediatrie|December 1, 1984
[Medium chain acyl-CoA dehydrogenase deficiency. Apropos of a case with demonstration of this enzyme deficiency]J P Collet, P Divry, J F Blanc, et al.
The Journal of Pediatrics|December 10, 1999
Primary hyperoxaluria in infants: medical, ethical, and economic issuesP Cochat, P C Koch Nogueira, M A Mahmoud, et al.
Kidney International|September 12, 1998
Body composition in children receiving recombinant human growth hormone after renal transplantationJ Feber, P Cochat, J Lebl, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 26, 2015
[Macrophage activation syndrome and autoimmunity due to visceral leishmaniasis]L Higel, C Froehlich, M-P Pages, et al.
Annals of Vascular Surgery|June 21, 2001
Surgical repair of an aneurysm of the innominate artery with fistulization into the tracheaJ P Guibaud, M N Laborde, J Dubrez, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|November 5, 1997
[Study of plasma acylcarnitines using tandem mass spectrometry. Application to the diagnosis of metabolism hereditary diseases]F Delolme, C Vianey-Saban, N Guffon, et al.
Pageof 32